Bassuoni Yasmine F, AboulMagd Asmaa M, Ibrahim Maha M
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Modern University for Technology and Information (MTI), 12582 Al Hadaba Al Wosta, Cairo, Egypt.
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Nahda University in Beni-Suef (NUB), Beni-Suef, 62513, Egypt.
BMC Chem. 2025 May 21;19(1):136. doi: 10.1186/s13065-025-01500-7.
Nowadays, one of the main objectives is to protect the environment and reduce the adverse impacts of chemicals on it. One of the most difficult issues for researchers is determining the efficiency and quality of the suggested approach in terms of environmental and human safety. The present research presents advanced, accurate, green high-performance liquid chromatographic method (HPLC) to estimate a combination of methocarbamol (MET) and aspirin (ASP) as well as their related impurities, guaifenesin (GUF) and salicylic acid (SA), respectively, with low retention time and ideal separation. Chromatographic separation was performed on X-Bridge C reversed phase (RP) column (4.6 × 250 mm, 5 μm particle size) utilizing methanol: water: triethylamine (70:30, 0.1% by volume) at pH 3.00 by o-phosphoric acid as a mobile phase with 2.00 mL min flow rate at 254.00 nm. The proposed method succeeded to achieve linearity over a concentration ranges of 0.30-50.00 μg mL, 1.00-300.00 μg mL, 10.00-500.00 μg mL and 0.10-50.00 μg mL for GUF, MET, ASP and SA, respectively. All the developed results were validated in compliance with the International Council of Harmonization (ICH) instructions. The suggested method was successfully applied to assess MET and ASP in their pharmaceutical formulation and in spiked human plasma. The molecular docking approach was employed to evaluate how the two drugs and their related impurities interacted with the stationary phase and to predict the suggested sequence of elution. The greenness of the developed analytical method was evaluated using whiteness assessment and two green approaches; analytical eco-scale and AGREE. The proposed method proved not only to be green, time-saving and more sensitive for the routine analysis of MET and ASP in QC laboratories, but also it can effectively handle the presence of impurities such as GUF and SA.
如今,主要目标之一是保护环境并减少化学品对环境的不利影响。对研究人员来说,最困难的问题之一是从环境和人类安全的角度确定所建议方法的效率和质量。本研究提出了先进、准确的绿色高效液相色谱法(HPLC),分别用于测定美索巴莫(MET)和阿司匹林(ASP)及其相关杂质愈创甘油醚(GUF)和水杨酸(SA)的组合,具有低保留时间和理想的分离效果。色谱分离在X-Bridge C反相(RP)柱(4.6×250 mm,粒径5μm)上进行,以甲醇:水:三乙胺(70:30,体积分数0.1%)为流动相,用邻磷酸调节pH至3.00,流速为2.00 mL/min,检测波长为254.00 nm。所提出的方法成功实现了在0.30 - 50.00μg/mL、1.00 - 300.00μg/mL、10.00 - 500.00μg/mL和0.10 - 50.00μg/mL浓度范围内分别对GUF、MET、ASP和SA的线性关系。所有得出的结果均按照国际协调理事会(ICH)的指导原则进行了验证。所建议的方法成功应用于评估其药物制剂和加标人血浆中的MET和ASP。采用分子对接方法评估这两种药物及其相关杂质与固定相的相互作用方式,并预测所建议的洗脱顺序。使用白度评估和两种绿色方法(分析生态规模和AGREE)对所开发分析方法的绿色度进行了评估。所提出的方法不仅被证明对质量控制实验室中MET和ASP的常规分析具有绿色、省时和更灵敏的特点,而且还能有效处理GUF和SA等杂质的存在。